Wawa Chocolate Low-fat Milk 16 oz , (Pint) Plastic bottle .Store Refrigerated
Summary
The FDA issued a Class II for Wawa Chocolate Low-fat Milk 16 oz , (Pint) Plastic bottle .Store Refrigerated by Wawa Beverage Company. Reason: Foreign plastic material discovered on fill line..
Details
Source
Food Recall
External ID
H-0588-2026
Action Date
2026-03-25
Status
Terminated
Category
food
Product Description
Wawa Chocolate Low-fat Milk 16 oz , (Pint) Plastic bottle .Store Refrigerated
Lot/Code Info: UPC: 00726191014908
Quantity Affected: 5456 units total
Reason for Recall
Foreign plastic material discovered on fill line.
Distribution
The recalled product was distributed to the following States: NJ,MD, DE, PA
Type: Voluntary: Firm initiated
Recall Initiated: 2026-02-17
Company
Media, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 48 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Wawa Beverage Company has 11 FDA actions in our database, including 11 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Wawa Beverage Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wawa Beverage Company have FDA actions?
Wawa Beverage Company has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0588-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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